lysine has been researched along with Smith-Lemli-Opitz Syndrome in 1 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ki, CS; Kim, JW | 1 |
1 other study(ies) available for lysine and Smith-Lemli-Opitz Syndrome
| Article | Year |
|---|---|
Identification of a novel DHCR7 mutation in a Korean patient with Smith-Lemli-Opitz syndrome.
Topics: Arginine; DNA Mutational Analysis; Female; Humans; Infant; Korea; Lysine; Mutation; Oxidoreductases Acting on CH-CH Group Donors; Smith-Lemli-Opitz Syndrome | 2007 |